Published April 1, 2015 | Version v1
Journal article

Phase 1/2 Trials of Temozolomide, Motexafin Gadolinium, and 60-Gy Fractionated Radiation for Newly Diagnosed Supratentorial Glioblastoma Multiforme: Final Results of RTOG 0513

  • 1. Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona (United States)
  • 2. Arizona Oncology Services Foundation, Scottsdale, Arizona (United States)
  • 3. Radiation Therapy Oncology Group Statistical Center, Philadelphia, Pennsylvania (United States)
  • 4. University of Florida College of Medicine, Gainesville, Florida (United States)
  • 5. St. Joseph Mercy Hospital, Ann Arbor, Michigan (United States)
  • 6. University of Wisconsin Hospital, Madison, Wisconsin (United States)
  • 7. Medical College of Wisconsin, Milwaukee, Wisconsin (United States)
  • 8. University of Washington Medical Center, Seattle, Washington (United States)
  • 9. Emory University, Atlanta, Georgia (United States)

Description

Purpose: The purpose of phase 1 was to determine the maximum tolerated dose (MTD) of motexafin gadolinium (MGd) given concurrently with temozolomide (TMZ) and radiation therapy (RT) in patients with newly diagnosed supratentorial glioblastoma multiforme (GBM). Phase 2 determined whether this combination improved overall survival (OS) and progression-free survival (PFS) in GBM recursive partitioning analysis class III to V patients compared to therapies for recently published historical controls. Methods and Materials: Dose escalation in phase 1 progressed through 3 cohorts until 2 of 6 patients experienced dose-limiting toxicity or a dose of 5 mg/kg was reached. Once MTD was established, a 1-sided 1-sample log-rank test at significance level of .1 had 85% power to detect a median survival difference (13.69 vs 18.48 months) with 60 deaths over a 12-month accrual period and an additional 18 months of follow-up. OS and PFS were estimated using the Kaplan-Meier method. Results: In phase 1, 24 patients were enrolled. The MTD established was 5 mg/kg, given intravenously 5 days a week for the first 10 RT fractions, then 3 times a week for the duration of RT. The 7 patients enrolled in the third dose level and the 94 enrolled in phase 2 received this dose. Of these 101 patients, 87 were eligible and evaluable. Median survival time was 15.6 months (95% confidence interval [CI]: 12.9-17.6 months), not significantly different from that of the historical control (P=.36). Median PFS was 7.6 months (95% CI: 5.7-9.6 months). One patient (1%) experienced a grade 5 adverse event possibly related to therapy during the concurrent phase, and none experience toxicity during adjuvant TMZ therapy. Conclusions: Treatment was well tolerated, but median OS did not reach improvement specified by protocol compared to historical control, indicating that the combination of standard RT with TMZ and MGd did not achieve a significant survival advantage

Availability note (English)

Available from http://dx.doi.org/10.1016/j.ijrobp.2014.12.050

Additional details

Identifiers

DOI
10.1016/j.ijrobp.2014.12.050;
PII
S0360-3016(14)04564-7;

Publishing Information

Journal Title
International Journal of Radiation Oncology, Biology and Physics
Journal Volume
91
Journal Issue
5
Journal Page Range
p. 961-967
ISSN
0360-3016
CODEN
IOBPD3

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
47028245
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
COMPARATIVE EVALUATIONS; CONTROL; DEATH; DIAGNOSIS; GADOLINIUM; GLIOMAS; PATIENTS; RADIATION DOSES; RADIOTHERAPY; SURVIVAL TIME; TOXICITY
Descriptors DEC
DISEASES; DOSES; ELEMENTS; EVALUATION; MEDICINE; METALS; NEOPLASMS; NERVOUS SYSTEM DISEASES; NUCLEAR MEDICINE; RADIOLOGY; RARE EARTHS; THERAPY

Optional Information

Copyright
Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.